Glycosylamines contain the easily cleavable semi-aminal-type N-glycosidic bond. O-Protected glycosylamines, therefore, can advantageously be used as a form of "asymmetric ammonia", for instance, in Strecker syntheses and in Ugi reactions to give amino acid amides as well as in modifications of the Mannich reaction
Absrracr: By exploiting the selective hydrogen atom transfer reactions of glycine residues in small ...
(R)-Homoallyl amines are synthesized with high asymmetric induction using the diastereoselective Lew...
Mannich-type reactions are powerful methods for the efficient synthesis of beta-amino carbonyl compo...
Abstract: Enantiomerically pure homoallyl amines and ~amino acids are synthesized using the diastere...
The synthesis of C-glycosyl beta-amino acids by asymmetric Mannich-type three-component reactions is...
Carbohydrates are of enormous importance for chemical, biological and medicinal science, because the...
A new method for threo-selective synthesis of β-amino alcohols is described. This method employs N-d...
The stereoconservative Staudinger ligation of unprotected α- and β-glucosyl azides with diphenylphos...
The importance of carbohydrates for asymmetric synthesis is well recognized [1-4].The reason that ca...
Glycoproteins play an important role in biological processes including intercellular communication, ...
alfa -Glycosyl amides can be synthesised from the corresponding O-benzyl-alfa-glycosyl azides using ...
We have synthesised a novel oxanorbornene beta-aminoacid derivative and employed it in a stereoselec...
C-Galactosyl and C-ribosyl b-amino acids were prepared by one-pot InCl3-catalyzed Mannich-type three...
The stereoconservative Staudinger ligation of unprotected\u3b1- and \u3b2-glycosyl azides with 2-(di...
The development of new methods for the preparation of C-glycosyl b-amino acid libraries with chemi...
Absrracr: By exploiting the selective hydrogen atom transfer reactions of glycine residues in small ...
(R)-Homoallyl amines are synthesized with high asymmetric induction using the diastereoselective Lew...
Mannich-type reactions are powerful methods for the efficient synthesis of beta-amino carbonyl compo...
Abstract: Enantiomerically pure homoallyl amines and ~amino acids are synthesized using the diastere...
The synthesis of C-glycosyl beta-amino acids by asymmetric Mannich-type three-component reactions is...
Carbohydrates are of enormous importance for chemical, biological and medicinal science, because the...
A new method for threo-selective synthesis of β-amino alcohols is described. This method employs N-d...
The stereoconservative Staudinger ligation of unprotected α- and β-glucosyl azides with diphenylphos...
The importance of carbohydrates for asymmetric synthesis is well recognized [1-4].The reason that ca...
Glycoproteins play an important role in biological processes including intercellular communication, ...
alfa -Glycosyl amides can be synthesised from the corresponding O-benzyl-alfa-glycosyl azides using ...
We have synthesised a novel oxanorbornene beta-aminoacid derivative and employed it in a stereoselec...
C-Galactosyl and C-ribosyl b-amino acids were prepared by one-pot InCl3-catalyzed Mannich-type three...
The stereoconservative Staudinger ligation of unprotected\u3b1- and \u3b2-glycosyl azides with 2-(di...
The development of new methods for the preparation of C-glycosyl b-amino acid libraries with chemi...
Absrracr: By exploiting the selective hydrogen atom transfer reactions of glycine residues in small ...
(R)-Homoallyl amines are synthesized with high asymmetric induction using the diastereoselective Lew...
Mannich-type reactions are powerful methods for the efficient synthesis of beta-amino carbonyl compo...